Rubnitz JE - Search Results

1

The genetic basis and cell of origin of mixed phenotype acute leukaemia.

Alexander TB, Gu Z, Iacobucci I, Dickerson K, Choi JK, Xu B, Payne-Turner D, Yoshihara H, Loh ML, Horan J, Buldini B, Basso G, Elitzur S, de Haas V, Zwaan CM, Yeoh A, Reinhardt D, Tomizawa D, Kiyokawa N, Lammens T, De Moerloose B, Catchpoole D, Hori H, Moorman A, Moore AS, Hrusak O, Meshinchi S, Orgel E, Devidas M, Borowitz M, Wood B, Heerema NA, Carrol A, Yang YL, Smith MA, Davidsen TM, Hermida LC, Gesuwan P, Marra MA, Ma Y, Mungall AJ, Moore RA, Jones SJM, Valentine M, Janke LJ, Rubnitz JE, Pui CH, Ding L, Liu Y, Zhang J, Nichols KE, Downing JR, Cao X, Shi L, Pounds S, Newman S, Pei D, Guidry Auvil JM, Gerhard DS, Hunger SP, Inaba H, Mullighan CG. Alexander TB, et al. Among authors: rubnitz je. Nature. 2018 Oct;562(7727):373-379. doi: 10.1038/s41586-018-0436-0. Epub 2018 Sep 12. Nature. 2018. PMID: 30209392 Free PMC article.

2

11q23 rearrangements in acute leukemia.

Rubnitz JE, Behm FG, Downing JR. Rubnitz JE, et al. Leukemia. 1996 Jan;10(1):74-82. Leukemia. 1996. PMID: 8558942 Review.

3

TEL/AML1 fusion resulting from a cryptic t(12;21) is the most common genetic lesion in pediatric ALL and defines a subgroup of patients with an excellent prognosis.

Shurtleff SA, Buijs A, Behm FG, Rubnitz JE, Raimondi SC, Hancock ML, Chan GC, Pui CH, Grosveld G, Downing JR. Shurtleff SA, et al. Among authors: rubnitz je. Leukemia. 1995 Dec;9(12):1985-9. Leukemia. 1995. PMID: 8609706

4

Molecular analysis of t(11;19) breakpoints in childhood acute leukemias.

Rubnitz JE, Behm FG, Curcio-Brint AM, Pinheiro RP, Carroll AJ, Raimondi SC, Shurtleff SA, Downing JR. Rubnitz JE, et al. Blood. 1996 Jun 1;87(11):4804-8. Blood. 1996. PMID: 8639852 Free article.

5

High incidence of TEL/AML1 fusion resulting from a cryptic t(12;21) in childhood B-lineage acute lymphoblastic leukemia in Taiwan.

Liang DC, Chou TB, Chen JS, Shurtleff SA, Rubnitz JE, Downing JR, Pui CH, Shih LY. Liang DC, et al. Among authors: rubnitz je. Leukemia. 1996 Jun;10(6):991-3. Leukemia. 1996. PMID: 8667657

6

Lack of TEL-AML1 fusion transcript resulting from a cryptic t(12;21) in adult B lineage acute lymphoblastic leukemia in Taiwan.

Shih LY, Chou TB, Liang DC, Tzeng YS, Rubnitz JE, Downing JR, Pui CH. Shih LY, et al. Among authors: rubnitz je. Leukemia. 1996 Sep;10(9):1456-8. Leukemia. 1996. PMID: 8751462

7

Case-control study suggests a favorable impact of TEL rearrangement in patients with B-lineage acute lymphoblastic leukemia treated with antimetabolite-based therapy: a Pediatric Oncology Group study.

Rubnitz JE, Shuster JJ, Land VJ, Link MP, Pullen DJ, Camitta BM, Pui CH, Downing JR, Behm FG. Rubnitz JE, et al. Blood. 1997 Feb 15;89(4):1143-6. Blood. 1997. PMID: 9028935 Free article. Clinical Trial.

8

TEL gene rearrangement in acute lymphoblastic leukemia: a new genetic marker with prognostic significance.

Rubnitz JE, Downing JR, Pui CH, Shurtleff SA, Raimondi SC, Evans WE, Head DR, Crist WM, Rivera GK, Hancock ML, Boyett JM, Buijs A, Grosveld G, Behm FG. Rubnitz JE, et al. J Clin Oncol. 1997 Mar;15(3):1150-7. doi: 10.1200/JCO.1997.15.3.1150. J Clin Oncol. 1997. PMID: 9060558

9

Lack of ETV6 (TEL) gene rearrangements or p16INK4A/p15INK4B homozygous gene deletions in infant acute lymphoblastic leukemia.

Maloney KW, Rubnitz JE, Cleary ML, Frankel LS, Hakami N, Link MP, Pullen DJ, Hunger SP. Maloney KW, et al. Among authors: rubnitz je. Leukemia. 1997 Jul;11(7):979-83. doi: 10.1038/sj.leu.2400687. Leukemia. 1997. PMID: 9204978

10

Recent advances in the biology and treatment of childhood acute lymphoblastic leukemia.

Rubnitz JE, Pui CH. Rubnitz JE, et al. Curr Opin Hematol. 1997 Jul;4(4):233-41. doi: 10.1097/00062752-199704040-00003. Curr Opin Hematol. 1997. PMID: 9260050 Review.

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